Rett Syndrome

Author:

Negi Namrata1

Affiliation:

1. Kol Valley Institute of Nursing, Village Nehar Harnora, Bilaspur (H.P).

Abstract

Rett syndrome is a rare developmental disorder which affects the brain development and the symptoms grows as the age progresses. It is first seen at the age of 6-18 months and predominantly seen in females; cases with male children are limited. 95% of the Rett syndrome cases are known to be due to mutation in MeCP2 genes present in the X chromosome. Approximately 3, 50,000 cases have been reported worldwide and the cases are growing. In India, 6 cases of Rett syndrome were encountered in the year 1992 and 1993 but was misdiagnosed; correctly reported in the year 1994. The cure is unknown for the syndrome but multidisciplinary approach helps in addressing the symptoms effectively.

Publisher

A and V Publications

Subject

General Medicine

Reference12 articles.

1. About Rett Syndrome; Available at - https://reverserett.org/about-rett-syndrome/

2. EEJ Smeets et al. Rett Syndrome. Molecular syndeomology .2011;2:113-127 doi: 10.1159/000337637 Available at -https://www.karger.com/Article/Pdf/337637

3. Shervin Pejhan, Mojgan Rastegar. Role of DNA Methyl –CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.biomolecules.2021;11(1):75 doi: http://doi.org/10.3390/biom11010075 Available at https://www.mdpi.com/2218-273X/11/1/75

4. Rett Syndrome. Available at -https://www.rettsyndrome.org/about-rett-syndrome/what-is-rett-syndrome/

5. Types of Rett Syndrome. Available at - https://rettsyndromenews.com/types-of-rett-syndrome/

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